Polyester synthase and a gene coding for the same

ABSTRACT

The present invention relates to a polypeptide comprising the amino acid sequence of SEQ ID NO:1 or a sequence of SEQ ID NO:1 where in one or more amino acids are deleted, replaced or added, and the polypeptide having polyester synthase activity; a polyester synthase gene comprising DNA coding for the above polypeptide; a recombinant vector comprising the gene; and a transformant transformed with the recombinant vector is also provided.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation-in-part, and claims the benefit of priority under 35 USC §120, of U.S. application Ser. No. 09/052,339, filed Mar. 30, 1998, now U.S. Pat. No. 5,968,805 which claims the benefit under 35 U.S.C. §119 of Japanese patent application no. 82965/1977, filed Apr. 1, 1997. The disclosure of the prior applications are considered part of (and are incorporated by reference in) the disclosure of this application.

FIELD OF THE INVENTION

The present invention relates to polyester synthase, a gene coding for the enzyme, a recombinant vector containing the gene, a transformant transformed with the vector, and a process for producing polyester synthase by use of the transformant.

BACKGROUND OF THE INVENTION

Polyesters (e.g., poly-3-hydroxyalkanoic acid) biosynthesized by microorganisms are biodegradable plastics with thermoplasticity ranging widely from rigid matter to viscoelastic rubber.

Poly-3-hydroxybutanoic acid (P(3HB)) is a typical polyester consisting of C4 monomer units, but it is a rigid and brittle polymeric material, so its application is limited. Accordingly, various polyesters such as P(3HB-co-3HV) having (P(3HB)) copolymerized with a C5 monomer unit (3HV) by adding propionic acid etc. to the medium have been prepared and examined to alter the physical properties of the polyester. On the other hand, polyesters consisting of at least C6 monomer units are soft polymeric materials having plasticity.

Polyester-synthesizing microorganisms are roughly divided into 2 groups, that is, those synthesizing polyesters with C3-5 monomer units and those synthesizing polyesters with C6-14 monomer units. The former microorganisms possess a polyester synthase using C3-5 monomer units as the substrate, while the latter microorganisms possess a polyester synthase using C6-14 monomer units as the substrate. Therefore, polyesters with different properties are synthesized by the respective microorganisms.

However, the respective polyesters from such known microorganisms are different in substrate specificity, so with one kind of enzyme given, polyesters (copolymers) having various monomer unit compositions adapted to the object of use are difficult to synthesize.

SUMMARY OF THE INVENTION

The object of the present invention is to provide a polyester synthase with monomer units having a wide range of carbon atoms as the substrate, a gene coding for the enzyme, a recombinant vector containing the gene, a transformant transformed with the vector, and a process for producing the polyester synthase by use of the transformant.

As a result of their eager research, the present inventors succeeded in cloning a polyester synthase gene from a microorganism belonging to the genus Pseudomonas isolated from soil, to arrive at the completion of the present invention.

That is, the present invention is a polypeptide comprising the amino acid sequence of SEQ ID NO:1 or a sequence where in said amino acid sequence, one or more amino acids are deleted, replaced or added, said polypeptide having polyester synthase activity.

Further, the present invention is a polyester synthase gene comprising DNA coding for said polypeptide. The DNA coding for the protein with polyester synthase activity includes, e.g., that of SEQ ID NO:2.

Further, the present invention is a polyester synthase gene comprising the nucleotide sequence of SEQ ID NO:3.

Further, the present invention is a recombinant vector comprising the polyester synthase gene.

Further, the present invention is a transformant transformed with said recombinant vector.

Further, the present invention is a process for producing polyester synthase wherein said transformant is cultured in a medium and polyester synthase is recovered from the resulting culture.

DETAILED DESCRIPTION OF THE INVENTION

Hereinafter, the present invention is described in detail.

(1) Cloning Of The Polyester Synthase Gene

The polyester synthase gene of the present invention is separated from a microorganism belonging to the genus Pseudomonas.

First, genomic DNA is isolated from a strain having the polyester synthase gene. Such a strain includes, e.g., Pseudomonas sp. Any known methods can be used for preparation of genomic DNA. For example, Pseudomonas sp. is cultured in a bouillon medium and then its genomic DNA is prepared by the hexadecyl trimethyl ammonium bromide method (Current Protocols in Molecular Biology, vol. 1, page 2.4.3., John Wiley & Sons Inc., 1994).

The DNA obtained in this manner is partially digested with a suitable restriction enzyme (e.g., Sau3AI, BamHI, BglII etc.). It is then ligated into a vector dephosphorylated by treatment with alkaline phosphatase after cleavage with a restriction enzyme (e.g., BamHI, BglII etc.) to prepare a library.

Phage or plasmid capable of autonomously replicating in host microorganisms is used as the vector. The phage vector includes, e.g., EMBL3, M13, gt11 etc., and the plasmid vector includes, e.g., pBR322, pUC18, and pBluescript II (Stratagene). Vectors capable of autonomously replicating in 2 or more host cells such as E. coli and Bacillus brevis, as well as various shuttle vectors, can also be used. Such vectors are also cleaved with said restriction enzymes so that their fragment can be obtained.

Conventional DNA ligase is used to ligate the resulting DNA fragment into the vector fragment. The DNA fragment and the vector fragment are annealed and then ligated to produce a recombinant vector.

To introduce the recombinant vector into a host microorganism, any known methods can be used. For example, if the host microorganism is E. coli, the calcium chloride method (Lederberg, E. M. et al., J. Bacteriol. 119, 1072 (1974)) and the electroporation method (Current Protocols in Molecular Biology, vol. 1, page 1.8.4 (1994)) can be used. If phage DNA is used, the in vitro packaging method (Current Protocols in Molecular Biology, vol. 1, page 5.7.1 (1994)) etc. can be adopted. In the present invention, an in vitro packaging kit (Gigapack II, produced by Stratagene etc.) may be used.

To obtain a DNA fragment containing the polyester synthase gene derived from Pseudomonas sp., a probe is then prepared. The amino acid sequences of some polyester synthases have already been known (Peoples, O. P. and Sinskey, A. J., J. Biol. Chem., 264, 15293 (1989); Huisman, G. W. et al., J. Biol. Chem., 266, 2191 (1991); Pieper, U. et al., FEMS Microbiol. Lett., 96, 73 (1992); Timm, A. and Steinbuchel, A., Eur. J. Biochem., 209, 15 (1992), etc.). Well-conserved regions are selected from these amino acid sequences, and nucleotide sequences coding for them are estimated to design oligonucleotides. Examples of such oligonucleotides include, but are not limited to, the sequence 5′-CC(G/C)CAGATCAACAAGTT(C/T)TA(C/G)GAC-3′ (SEQ ID NO:4) reported by Timm, A. and Steinbuchel, A., Eur. J. Biochem., 209, 15 (1992).

Then, this synthetic oligonucleotide is labeled with a suitable reagent and used for colony hybridization of the above genomic DNA library (Current Protocols in Molecular Biology, vol. 1, page 6.0.3 (1994)).

The E. coli is screened by colony hybridization, and a plasmid is recovered from it using the alkaline method (Current Protocols in Molecular Biology, vol. 1, page 1.6.1 (1994)), whereby a DNA fragment containing the polyester synthase gene is obtained. The nucleotide sequence of this DNA fragment can be determined in, e.g., an automatic nucleotide sequence analyzer such as 373A DNA sequencer (Applied Biosystems) using a known method such as the Sanger method (Molecular Cloning, vol. 2, page 13.3 (1989)).

After the nucleotide sequence was determined by the means described above, the gene of the present invention can be obtained by chemical synthesis or the PCR technique using genomic DNA as a template, or by hybridization using a DNA fragment having said nucleotide sequence as a probe.

(2) Preparation of Transformant

The transformant of the present invention is obtained by introducing the recombinant vector of the present invention into a host compatible with the expression vector used in constructing said recombinant vector.

The host is not particularly limited insofar as it can express the target gene. Examples are bacteria such as microorganisms belonging to the genus Alcaligenes, microorganisms belonging to the genus Bacillus, bacteria such as E. coli, yeasts such as the genera Saccharomyces, Candida etc., and animal cells such as COS cells, CHO cells etc.

If microorganisms belonging to the genus Alcaligenes or bacteria such as E. coli are used as the host, the recombinant DNA of the present invention is preferably constituted such that it contains a promoter, the DNA of the present invention, and a transcription termination sequence so as to be capable of autonomous replication in the host. The expression vector includes pLA2917 (ATCC 37355) containing replication origin RK2 and pJRD215 (ATCC 37533) containing replication origin RSF1010, which are replicated and maintained in a broad range of hosts.

The promoter may be any one if it can be expressed in the host. Examples are promoters derived from E. coli, phage etc., such as trp promoter, lac promoter, PL promoter, PR promoter and T7 promoter. The method of introducing the recombinant DNA into bacteria includes, e.g., a method using calcium ions (Current Protocols in Molecular Biology, vol. 1, page 1.8.1 (1994)) and the electroporation method (Current Protocols in Molecular Biology, vol. 1, page 1.8.4 (1994)).

If yeast is used as the host, expression vectors such as YEp13, YCp50 etc. are used. The promoter includes, e.g., gal 1 promoter, gal 10 promoter etc. To method of introducing the recombinant DNA into yeast includes, e.g., the electroporation method (Methods. Enzymol., 194, 182-187 (1990)), the spheroplast method (Proc. Natl. Acad. Sci. USA, 84, 1929-1933 (1978)), the lithium acetate method (J. Bacteriol., 153, 163-168 (1983)) etc.

If animal cells are used as the host, expression vectors such as pcDNAI, pcDNAI/Amp (produced by Invitrogene) etc. are used. The method of introducing the recombinant DNA into animal cells includes, e.g., the electroporation method, potassium phosphate method etc.

(3) Production of polyester Synthase

Production of the polyester synthase of the present invention is carried out by culturing the transformant of the present invention in a medium, forming and accumulating the polyester synthase of the present invention in the culture (the cultured microorganism or the culture supernatant) and recovering the polyester synthase from the culture.

A conventional method used for culturing the host is also used to culture the transformant of the present invention.

The medium for the transformant prepared from bacteria cush as E. coli etc. as the host includes complete medium or synthetic medium, e.g. LB medium, M9 medium etc. The transformant is aerobically cultured at a temperature ranging from 25 to 37 degrees C. for 12 to 48 hours so that the polyester synthase is accumulated in the microorganism and then recovered.

The carbon source is essential for the growth of the microorganism and includes, e.g., carbohydrates such as glucose, fructose, sucrose, maltose etc.

The nitrogen source includes, e.g., ammonia, ammonium salts such as ammonium chloride, ammonium sulfate, ammonium phosphate etc., peptone, meat extract, yeast extract, corn steep liquor etc. The inorganic matter includes, e.g., monopotassium phosphate, dipotassium phosphate, magnesium phosphate, magnesium sulfate, sodium chloride etc.

Culture is carried out usually under aerobic conditions with shaking at 25 to 37° C. for more than 2 hours after expression is induced. During culture, antibiotics such as ampicillin, kanamycin, ampicillin, tetracycline etc. may be added to the culture.

To culture the microorganism transformed with the expression vector using an inducible promoter, its inducer can also be added to the medium. For example, isopropyl-D-thiogalactopyranoside (IPTG), indoleacrylic acid (IAA) etc. can be added to the medium.

To culture the transformant from animal cells as the host, use is made of a medium such as RPMI-1640 or DMEM which may be supplemented with fetal bovine serum. Culture is carried out usually in 5% CO2 at 30 to 37° C. for 1 to 7 days. During culture, antibiotics such as kanamycin, penicillin etc. may be added to the medium.

Purification of the polyester synthase can be performed by recovering the resulting culture by centrifugation (after disruption in the case of cells) and subjecting it to affinity chromatography, cation or anion exchange chromatography or gel filtration or to a suitable combination thereof.

Whether the resulting purified substance is the desired enzyme is confirmed by conventional methods such as SDS polyacrylamide gel electrophoresis, Western blotting etc.

EXAMPLES

Hereinafter, the present invention is described in more detail with reference to the Examples, which, however are not intended to limit the scope of the present invention.

Example 1

(1) Cloning of the Polyester Synthase Gene From Pseudomonas sp.

First, a genomic DNA library of Pseudomonas sp. was prepared.

Pseudomonas sp. JCM 10015 was cultured overnight in 100 ml bouillon medium (1% meat extract, 1% peptone, 0.5% sodium chloride, pH 7.2) at 30° C. and then genomic DNA was obtained from the microorganism using the hexadecyl trimethyl ammonium bromide method (Current Protocols in Molecular Biology, vol. 1, page 2.4.3 (1994), John Wiley & Sons Inc.).

The resulting genomic DNA was partially digested with restriction enzyme Sau3AI. The vector plasmid used was cosmid vector pLA2917 (ATCC 37355). This plasmid was cleaved with restriction enzyme BglII and dephosphorylated (Molecular Cloning, vol. 1, page 5.7.2 (1989), Cold Spring Harbor Laboratory) and then ligated into the partially digested genomic DNA fragment by use of DNA ligase.

E. coli S 17-1 was transformed with this ligated DNA fragment by the in vitro packaging method (Current Protocols in Molecular Biology, vol. 1, page 5.7.2 (1994)) whereby a genomic DNA library from Pseudomonas sp. was obtained.

To obtain a DNA fragment containing the polyester synthase gene from Pseudomonas sp., a probe was then prepared. An oligonucleotide consisting of the sequence 5′-CC(G/C)CAGATCAACAAGTT(C/T)TA(C/G)GAC-3′ (SEQ ID NO:4) reported by Timm, A. and Steinbuchel, A., Eur. J. Biochem., 209, 15 (1992) was synthesized. This oligonucleotide was labeled with digoxigenin using a DIG DNA labeling kit (Boehringer Mannheim) and used as a probe.

Using the probe thus obtained, E. coli carrying a plasmid containing the polyester synthase gene was isolated by colony hybridization from the genomic DNA library from Pseudomonas sp.

When Alcaligenes eutrophus PHB-4 (DSM541) and Pseudomonas putida GPp104 (both of which are strains deficient in an ability to produce polyester) were transformed by the conjugation transfer method with the plasmid containing the polyester synthase gene, both the strains had a reverse ability to produce polyester and showed complementarity.

By recovering the plasmid from the E. coli, a DNA fragment containing the polyester synthase gene was obtained.

The nucleotide sequence of a PstI-XbaI fragment from this fragment was determined by the Sanger method.

As a result, the nucleotide sequence of the 1.8 kbp fragment shown in SEQ ID NO:3 was determined.

By further examining homology to this nucleotide sequence, the polyester synthase gene containing the nucleotide sequence (1680 bp) of SEQ ID NO:2 could be identified in this 1.8 kbp nucleotide sequence. The amino acid sequence encoded by SEQ ID NO:2 is shown in SEQ ID NO:1.

It should be understood that insofar as a protein containing the amino acid sequence of SEQ ID NO:1 or a sequence where in said amino acid sequence, one or more amino acids are deleted, replaced or added has polyester synthase activity, the gene (SEQ ID NO:2 or 3) containing DNA coding for said protein falls under the scope of the polyester synthase gene of the present invention.

Mutations such as deletion, replacement, addition etc. can be induced in the amino acid sequence or nucleotide sequence by the known site-direct mutagenesis method (e.g., Transfomer™ Site-Directed Mutagenesis Kit available from Toyobo).

(2) Preparation of E. coli Transformant

The 1.8 kb PstI-XbaI fragment containing the polyester synthase gene was ligated into the XbaI, PstI site of plasmid vector pBluescript II KS+. The resulting recombinant vector was transformed by the calcium chloride method into Escherichia coli DH5 . The resulting transformant was designated Escherichia coli PX18. By extracting the plasmid from this transformant, the 1.8 kb PstI-Xbal fragment containing the polyester synthase gene can be easily obtained. Escherichia coli PX18 has been deposited as FERM BP-6297 with the National Institute of Bioscience and Human-Technology, Agency of Industrial Science and Technology, Japan.

According to the present invention, there are provided a gene coding for polyester synthase, a recombinant vector containing the gene, and a transformant transformed with the vector. The gene of the present invention codes for a polyester synthase using monomers having a wide range of carbon atoms as the substrate, so it is useful in preparing copolymer polyesters having various physical properties.

Example 2

Introduction

Two types of polyhydroxyalkanoate biosynthesis gene loci (phb andpha) of Pseudomonas sp. 61-3 (JCM 10015), which produces a blend of poly(3-hydroxybutyrate) homopolymer [P(3HB)] and a random copolymer (poly(3-hydroxybutyrate-co-3-hydroxyalkanoates) [P(3HB-co-3HA]) consisting of 3HA units from 4 to 12 carbon numbers, were cloned and analyzed at the molecular level. In the present invention, the substrate specificities of PHA synthases were also evaluated by heterologous expression in PHA-negative mutant of R. eutropha.

Materials and Methods

Bacterial strains, plasmids, and growth conditions. Bacterial strains and plasmids used in this study are listed in Table 1, and the DNA fragments on vectors are illustrated in FIG. 1. Pseudomonas sp. 61-3 and R. eutropha strains were cultivated at 30° C. in a nutrient-rich (NR) medium containing 10 g of meat extract, 10 g of bactopeptone (Difco), and 2 g of yeast extract (Difco) in 1 liter of distilled water. Escherichia coli strains were grown at 37° C. on Luria-Bertani (LB) medium (9). When needed, kanamycin (50 mg/liter), tetracycline (12.5 mg/liter), or ampicillin (50 mg/liter) was added to the medium.

DNA manipulations. Isolation of total genomic DNA and plasmids, digestion of DNA with restriction endonucleases, agarose gel electrophoresis, and transformation of E. coli were carried out according to standard procedures (11) or the manufacturers. DNA restriction fragments were isolated from agarose gels by using QIAEX II Gel Extraction Kit (QIAGEN). All other DNA-manipulating enzymes were used as recommended by the manufacturers. Genomic DNA libraries of Pseudomonas sp. 61-3 were constructed with Charomid 9-28 (Nippon gene) and pLA2917 (2) by in vitro packaging using Gigapack II (Stratagene). Conjugation of R. eutropha with E. coli S17-1 harboring broad-host-range plasmids was performed as described by Friedrich et al. (4).

Plasmid construction. Plasmids pJASc22, pJASc60, and pJASc60dC1Z, were constructed as follows: The 2.2-kbp EcoRI-XbaI region containing a gene of the present invention (hereinafter referred to as phaC1_(Ps)), and the 6.0-kbp EcoRI-PstI region containing phaC1ZC2D_(Ps) were introduced into pJRD215 as 2.2-kbp and 6.0-kbp Apal-SacI fragments, to form pJASc22 and pJASc60, respectively (FIG. 1). A plasmid pJASc60dC1Z containing phaC2D_(Ps) was constructed by eliminating a BglII-SphI region from a pBluescript II KS+ derivative plasmid carrying the 6.0-kbp EcoRI-PstI region, and introducing the deleted fragment into pJRD215 at the ApaI and SacI sites (FIG. 1).

Plasmids pJASc50 and pJASc50dC1Z were constructed as follows: The 5.1-kbp EcoRI-BamHI region containing phaC1ZC2_(Ps) was introduced into pJRD215 as a 5.1-kbp ApaI-SacI fragment to form pJASc50 (FIG. 1). A plasmid pJASc50dC1Z containing a gene of the present invention (hereinafter referred to as phaC2_(Ps)) was constructed by eliminating a BglII-SphI region from a pBluescript II KS+ derivative plasmid carrying the 5.1 -kbp EcoRI-BamHI region, and introducing the deleted fragment into pJRD215 at the ApaI and SacI sites (FIG. 1).

Hybridization experiments. Hybridization was carried out as described by Southern (17). The DNA probes used were a 24-mer synthetic oligonucleotide, 5′-CC(G/C)CAGATCA ACAAG TT(C/T)TA(C/G)GAC-3′(SEQ ID NO 7), whose sequence was based on that of a highly conserved region of the polyester synthases of R. eutropha and P. oleovorans as described by Timm and Steinbühel (16). Preparation of digoxigenin-labeled probes and the detection of hybridization signals on membranes were carried out with DIG DNA Labeling and Detection Kit (Boehringer Mannheim) and DIG Oligonucleotide Tailing Kit (Boehringer Mannheim).

Nucleotide sequence analysis. DNA fragments to be sequenced were subcloned into pBluescript II KS+. DNA was sequenced by the modified dideoxy chain-termination method basically as described by Sanger et al. (18) with a 310 Genetic Analyzer (Perkin Elmer). The sequencing reaction was performed according to the manual supplied with the dye terminator cycle sequencing kit (Perkin Elmer). The resulting nucleotide sequence was analyzed with SDC-GENETYX genetic information processing software (Software Development Co., Tokyo, Japan).

Production and analysis of pha. Cells were cultivated on a reciprocal shaker (130 strokes/min) at 30° C. for 72 h in 500-ml flasks containing 100 ml of a nitrogen-limited mineral salt (MS) medium, which consisted of 0.9 g of Na₂HPO₄ 12H₂O, 0.15 g of KH₂PO₄, 0.05 g of NH₄Cl, 0.02 g of MgSO₄ 7H₂O, and 0.1 ml of trace element solution (8). Filter-sterilized carbon sources were added to the medium as indicated in the text. Determination of cellular PHA content and composition by gas chromatography, isolation of the accumulated PHA, fractionation of the isolated polyesters with acetone, and nuclear magnetic resonance (NMR) analysis of polyesters, were carried out in a manner as described by Kato et al. (8, 9).

Results

Cloning and identification of phb and pha loci of Pseudomonas sp. 61-3. To identify the two possible types of polyester synthase genes in Pseudomonas sp. 61-3, genomic DNA fragments from digestion with several restriction enzymes were hybridized with two different gene probes. One probe is a 1.8-kbp fragment carrying phb synthase gene of R. eutropha (phbC_(Re)), and the other is a 24-mer synthetic oligonucleotide previously used for identification of pha synthase genes from pseudomonads (16). Southern hybridization analysis using each probe showed different patterns of strong signals (14-kbp HindIII-, 20-kbp EcoRI-, 30-kbp BamHI-, 3.5-kbp PstI-, and 6.3-kbp SacI-fragments with the phbC_(Re) probe, and 17-kbp HindIII-, 1.9-kbp EcoRI-, 16-kbp BamHI-, 3.2-kbp PstI-, and 19-kbp SacI-fragments with the 24-mer oligonucleotide probe). This suggested that the two types of polyester synthase genes are located on different DNA loci in Pseudomonas sp. 61-3.

For cloning of the polyester synthase gene hybridized with the phbC_(Re) and the oligonucleotide probes, a genomic sublibrary of 14-kbp HindIII fragments with a cosmid vector Charomid 9-28, and a total genomic DNA library with a cosmid vector pLA2917 (2) from partially digested genomic DNA using Sau3AI were constructed by in vitro packaging. Positive clones isolated by each hybridization screening were further analyzed by Southern hybridization, and a 6.0-kbp HindIII-ApaI and a 6.0-kbp EcoRI-PstI regions were mapped, respectively.

Organization of phb and pha loci. The complete nucleotide sequences of the cloned fragments were determined in both strands. In the 6.0-kbp HindIII-ApaI region (phb locus), four potential open reading frames (ORFs) were identified by computer analysis for protein-coding regions. The nucleotide sequence revealed homologies to genes encoding phb synthase (PhbC_(Ps)), β-ketothiolase (PhbA_(Ps)), and NADPH-dependent acetoacetyl-CoA reductase (PhbB_(Ps)) in R. eutropha (Table 2). The phb locus of Pseudomonas sp. 61-3 was constituted of phbBAC_(Ps) operon, which is a different organization from the corresponding operon in R. eutropha (phbCAB_(Re)).

In the region upstream of phbB_(Ps), another ORF (1,137 bp) was oriented in the opposite direction to the other three genes. The ORF was referred to as phbR_(Ps).

In the 6.0-kbp EcoRI-PstI region (pha locus; SEQ ID NO:8), there are several genes with a similar organization to pha loci of P. oleovorans (6) and P. aeruginosa (16). Two polyester synthase genes, referred to as phaC1_(Ps) (SEQ ID NO:2) and phaC2_(Ps) (SEQ ID NO:5), are represented as two large open reading frames in this region (FIG. 1). Amino acid sequences encoded by phaC1_(Ps) and phaC2_(Ps) are shown in SEQ ID NOS: 1 and 6, respectively. The two PHA synthases of Pseudomonas sp. 61-3 exhibited 53.2% identity each other, which is similar to the homology between the two synthases of P. oleovorans (6). Putative PHA depolymerase is encoded by phaZ_(Ps) located between phaC1_(Ps) and phaC2_(Ps) in Pseudomonas sp. 61-3. An ORF was also identified downstream of phaC2_(Ps) of which deduced amino acid sequence was similar to that of ORF3 of P. aeruginosa (Table 2) (16), then it was designated as phaD_(Ps). ORF1 upstream of phaC1_(Ps) was similar to the 3′-terminal region of ORF2 of P. aeruginosa (81.7% identity for the C-terminal 93 amino acids) (16). Two nucleotide sequences resembling the E. coli-35 to -10 consensus sequence of σ⁷⁰-dependent promoter and the E. coli -24 to -12 consensus sequence of σ⁵⁴-dependent promoter were found upstream of phaC1_(Ps), although their relevance has not been yet explored.

Complementation studies and heterologous expression. To confirm whether the cloned fragments have functionally active PHA biosynthesis genes, heterologous expression of the genes was investigated in the PHA-negative mutants, R. eutropha PHB 4 (12). Plasmids pJASc60, pJASc22, pJASc60dC1Z, pJASc50 and pJASc50dC1Z harboring the PHA synthase gene were constructed as described Materials and Methods section. These plasmids were mobilized from E. coli Si7-1 to R. eutropha PHB 4. The transconjugants were cultivated under nitrogen-limiting conditions in MS medium to promote the PHA biosynthesis from gluconate, octanoate, dodecanoate, or tetradecanoate as a sole carbon source, and were analyzed by gas chromatography to determine the content and composition of the accumulated PHA.

Table 3 shows the results of PHA accumulation in the recombinant strains of R. eutropha PHB 4. The plasmids, pJASc22, pJASc60, pJASc60dC1Z, pJASc50 and pJASc50dC1Z could complement the deficiency of polyester synthases in both the mutant strains, and conferred the ability to accumulate PHA on the hosts.

The recombinant strains of PHB 4 harboring pJASc60, pJASc22, pJASc60dC1Z, pJASc50 and pJASc50dC1Z produced P(3HB) homopolymer from gluconate, while the strains produced P(3HB-co-3HA) copolymer consisting of 3HA of C₄- to C₁₂-monomer units from octanoate, dodecanoate, or tetradecanoate with relatively high 3HB contents (Table 3). 3HB compositions of 30 to 70 mol % were incorporated into the copolymers synthesized by the strains harboring pJASc22, pJASc60dC1Z, pJASc50 and pJASc50dC1Z from the alkanoates (Table 3). Interestingly, PHB 4/pJASc60 produced copolymers composed of much higher 3HB fraction (about 90 mol % 3HB) from octanoate and tetradecanoate. In order to determine whether the polyesters synthesized by PHB 4 strains carrying PHA synthase genes from alkanoates are random copolymers or not, the parameter D values were calculated based on the sequence distribution of 3HB and 3HA units by ¹³C-NMR analysis as described by Kamiya et al. (7), which suggested that these polyesters are random copolymers of 3HB and 3HA units (1.4 to 1.6 of D values). As a consequence, both PhaC1_(Ps) and PhaC2_(Ps) of Pseudomonas sp. 61-3 were found to be able to incorporate a wide compositional range of 3HA units from C₄ to C₁₂ into the polyester.

Discussion

R. eutropha PHB 4 strain harboring phaC1_(Ps) and/or phaC2_(Ps) produced P(3HB-co-3HA) copolymers consisting of 3HA units of 4 to 12 carbon numbers from alkanoates. These results indicate that both PHA synthases of Pseudomonas sp. 61-3 are able to incorporate 3HB unit into the polyester as well as medium-chain-length 3HA units.

The results described here demonstrate that the polyester synthase gene of the present invention makes it be possible to synthesize P(3HB-co-3HA) random copolymer with a novel composition having a wide range of rigidity or placticity.

FIGURE LEGENDS

FIG. 1. Organization of pha loci in Pseudomonas sp. 61-3 and DNA fragments including pha locus on broad-host-range vector used in this study.

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TABLE 1 BACTERIAL STRAINS AND PLASMIDS USED IN THIS STUDY. Strain or Plasmid Relevant Characteristics Source Or Reference(s)^(a) Strains Pseudomonas sp. strain 61-3 Wild type JCM 10015 1, 8, 9 R. eutropha PHB 4 PHA-negative mutant of H16 DSM 541, 12 E. coli DHSα deoR endA1 gyrA96 hsdR17 (r_(K)− m_(K)+) relA1 supE thi-1 Clontech Δ (lacZYA-argFV169) Δ80ΔlacZΔM15F-λ- E. coli S17-1 recA and tra genes of plasmid RP4 integrated into 14 chromosome; auxotrophic for proline and thiamine Plasmids pLA2917 Cosmid; Km^(r) Tc^(r) RK2 replicon; Mob⁺ 2 pJRD215 Cosmid; Km^(r) Sm^(r) RSF1010 replicon; Mob⁺ 3 pBluescript II KS⁺ Ap^(r) lacPOZ T7 and T3 promoter Stratagene pJASc22 pJRD215 derivative; phaC1_(Ps) This study pJASc60 pJRD215 derivative; phaCl_(Ps) phaZ_(Ps) phaC2_(Ps) phaD_(Ps) This study pJASc60dC1Z pJRD215 derivative; phaC2_(Ps) phaD_(Ps) This study pJASc50 pJRD215 derivative; phaC1_(Ps) phaZ_(Ps) phaC2_(Ps) This study pJASc50dC1Z pJRD215 derivative; phaC2_(Ps) This study ^(a)JCM, Japan Collection of Microorganisms; DSM, Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH.

TABLE 2 HOMOLOGY OF THE PRODUCTS OF THE PHB AND PHA LOCI OF PSEUDOMONAS sp. STRAIN 61-3 TO PROTEINS OF OTHER BACTERIA Homology To Other Gene Products Gene Product Size of Putative Amino acid Designation Gene Product Designation^(a) identity (%) PhbR_(Ps) 42.3 OruR 25.7 PhbB_(Ps) 26.7 PhbB_(Re) 66.1 PhbA_(Ps) 40.6 PhbA_(Re) 65.8 PhbC_(Ps) 64.3 PhbC_(Re) 53.0 PhaC1_(Ps) 62.3 PhaC1_(Po) 83.7 PhaZ_(Ps) 31.7 PhaZ_(Po) 89.0 PhaC2_(Ps) 62.8 PhaC2_(Po) 74.8 PhaD_(Ps) 23.5 PhaD_(Pa) 77.2 OruR, transcriptional regulator for ornithine matabolism of P. aeruginosa(5); PhbB_(Re), PhbA_(Re), and PhbC_(Re), NADPH-dependent acetoacetyl-CoA reductase, β-ketothiolase, and PHB synthase of R. eutropha, respectively (10, 13, 15); PhaC1_(Po), PhaZ_(Po), and PhaC2_(Po), PHA synthase 1, PHA depolymerase, and PHA

TABLE 3 ACCUMULATION OF PHA BY RECOMBINANT R. EUTROPHA PHB 4 STRAINS HARBORING PHA BIOSYNTHESIS GENES OF PSEUDOMONAS sp. STRAIN 61-3^(a) Dry cell PHA PHA composition (mol %)^(b) Plasmid Weight Content 3HB 3HHx 3HO 3HD 3HDD 3H5DD (Relevant Markers) Substrate (g/l) (wt %) (C4) (C6) (C8) (C10) (C12) (C12′) pJASc60 Gluconate 0.85 12 100 0 0 0 0 0 (phaC1, phaZ, phaC2, phaD) Octanoate 0.84 6 92 0 8 0 0 0 Dodecanoate 0.30 6 100 0 0 0 0 0 Tetradecanoate 0.69 4 91 0 3 3 3 0 pJASc22 Gluconate 0.74 2 100 0 0 0 0 0 (phaC1) Octanoate 0.86 13 31 10 59 0 0 0 Dodecanoate 0.61 5 31 4 23 23 19 0 Tetradecanoate 0.97 14 46 4 21 18 11 0 PJASc60dC1Z Gluconate 0.92 20 100 0 0 0 0 0 (phaC2, phaD) Octanoate 0.74 4 50 7 43 0 0 0 Dodecanoate 0.34 1 51 0 9 13 27 0 Tetradecanoate 0.67 5 44 1 16 15 24 0 pJASc50 Gluconate 0.52 2 100 0 0 0 0 0 (phaC1, phaZ, phaC2) Tetradecanoate 0.78 6 62 2 16 13 7 0 pJASc50dC1Z Gluconate 0.98 11 100 0 0 0 0 0 (phaC2) Tetradecanoate 0.75 3 69 0 11 10 10 0 ^(a)Cells were cultivated at 30° C. for 72 h in MS medium containing the sodium salt of gluconate (2% wt/vol), octanoate (0.1% wt/vol × 5), dodecanoate, or tetradecanoate (0.5% wt/vol) as a sole carbon source. ^(b)3HB, 3-hydroxybutyrate; 3HHx, 3-hydroxyhexanoate; 3HO, 3-hydroxyoctanoate; 3HD, 3-hydroxy-decanoate; 3HDD, 3-hydroxydodecanoate; 3H5DD, 3-hydroxy-cis-5-dodecenoate.

8 1 559 PRT Pseudomonas 1 Met Ser Asn Lys Asn Ser Asp Asp Leu Asn Arg Gln Ala Ser Glu Asn 1 5 10 15 Thr Leu Gly Leu Asn Pro Val Ile Gly Leu Arg Gly Lys Asp Leu Leu 20 25 30 Thr Ser Ala Arg Met Val Leu Thr Gln Ala Ile Lys Gln Pro Ile His 35 40 45 Ser Val Lys His Val Ala His Phe Gly Ile Glu Leu Lys Asn Val Met 50 55 60 Phe Gly Lys Ser Lys Leu Gln Pro Glu Ser Asp Asp Arg Arg Phe Asn 65 70 75 80 Asp Pro Ala Trp Ser Gln Asn Pro Leu Tyr Lys Arg Tyr Leu Gln Thr 85 90 95 Tyr Leu Ala Trp Arg Lys Glu Leu His Asp Trp Ile Gly Asn Ser Lys 100 105 110 Leu Ser Glu Gln Asp Ile Asn Arg Ala His Phe Val Ile Thr Leu Met 115 120 125 Thr Glu Ala Met Ala Pro Thr Asn Ser Ala Ala Asn Pro Ala Ala Val 130 135 140 Lys Arg Phe Phe Glu Thr Gly Gly Lys Ser Leu Leu Asp Gly Leu Thr 145 150 155 160 His Leu Ala Lys Asp Leu Val Asn Asn Gly Gly Met Pro Ser Gln Val 165 170 175 Asp Met Gly Ala Phe Glu Val Gly Lys Ser Leu Gly Thr Thr Glu Gly 180 185 190 Ala Val Val Phe Arg Asn Asp Val Leu Glu Leu Ile Gln Tyr Arg Pro 195 200 205 Thr Thr Glu Gln Val His Glu Arg Pro Leu Leu Val Val Pro Pro Gln 210 215 220 Ile Asn Lys Phe Tyr Val Phe Asp Leu Ser Pro Asp Lys Ser Leu Ala 225 230 235 240 Arg Phe Cys Leu Ser Asn Asn Gln Gln Thr Phe Ile Val Ser Trp Arg 245 250 255 Asn Pro Thr Lys Ala Gln Arg Glu Trp Gly Leu Ser Thr Tyr Ile Asp 260 265 270 Ala Leu Lys Glu Ala Val Asp Val Val Ser Ala Ile Thr Gly Ser Lys 275 280 285 Asp Ile Asn Met Leu Gly Ala Cys Ser Gly Gly Ile Thr Cys Thr Ala 290 295 300 Leu Leu Gly His Tyr Ala Ala Leu Gly Glu Lys Lys Val Asn Ala Leu 305 310 315 320 Thr Leu Leu Val Ser Val Leu Asp Thr Thr Leu Asp Ser Gln Val Ala 325 330 335 Leu Phe Val Asp Glu Lys Thr Leu Glu Ala Ala Lys Arg His Ser Tyr 340 345 350 Gln Ala Gly Val Leu Glu Gly Arg Asp Met Ala Lys Val Phe Ala Trp 355 360 365 Met Arg Pro Asn Asp Leu Ile Trp Asn Tyr Trp Val Asn Asn Tyr Leu 370 375 380 Leu Gly Asn Glu Pro Pro Val Phe Asp Ile Leu Phe Trp Asn Asn Asp 385 390 395 400 Thr Thr Arg Leu Pro Ala Ala Phe His Gly Asp Leu Ile Glu Met Phe 405 410 415 Lys Asn Asn Pro Leu Val Arg Ala Asn Ala Leu Glu Val Ser Gly Thr 420 425 430 Pro Ile Asp Leu Lys Gln Val Thr Ala Asp Ile Tyr Ser Leu Ala Gly 435 440 445 Thr Asn Asp His Ile Thr Pro Trp Lys Ser Cys Tyr Lys Ser Ala Gln 450 455 460 Leu Phe Gly Gly Lys Val Glu Phe Val Leu Ser Ser Ser Gly His Ile 465 470 475 480 Gln Ser Ile Leu Asn Pro Pro Gly Asn Pro Lys Ser Arg Tyr Met Thr 485 490 495 Ser Thr Asp Met Pro Ala Thr Ala Asn Glu Trp Gln Glu Asn Ser Thr 500 505 510 Lys His Thr Asp Ser Trp Trp Leu His Trp Gln Ala Trp Gln Ala Glu 515 520 525 Arg Ser Gly Lys Leu Lys Lys Ser Pro Thr Ser Leu Gly Asn Lys Ala 530 535 540 Tyr Pro Ser Gly Glu Ala Ala Pro Gly Thr Tyr Val His Glu Arg 545 550 555 2 1680 DNA Pseudomonas 2 atgagtaaca agaatagcga tgacttgaat cgtcaagcct cggaaaacac cttggggctt 60 aaccctgtca tcggcctgcg tggaaaagat ctgctgactt ctgcccgaat ggttttaacc 120 caagccatca aacaacccat tcacagcgtc aagcacgtcg cgcattttgg catcgagctg 180 aagaacgtga tgtttggcaa atcgaagctg caaccggaaa gcgatgaccg tcgtttcaac 240 gaccccgcct ggagtcagaa cccactctac aaacgttatc tacaaaccta cctggcgtgg 300 cgcaaggaac tccacgactg gatcggcaac agcaaactgt ccgaacagga catcaatcgc 360 gctcacttcg tgatcaccct gatgaccgaa gccatggccc cgaccaacag tgcggccaat 420 ccggcggcgg tcaaacgctt cttcgaaacc ggcggtaaaa gcctgctcga cggcctcaca 480 catctggcca aggacctggt aaacaacggc ggcatgccga gccaggtgga catgggcgct 540 ttcgaagtcg gcaagagtct ggggacgact gaaggtgcag tggttttccg caacgacgtc 600 ctcgaattga tccagtaccg gccgaccacc gaacaggtgc atgagcgacc gctgctggtg 660 gtcccaccgc agatcaacaa gttttatgtg tttgacctga gcccggataa aagcctggcg 720 cgcttctgcc tgagcaacaa ccagcaaacc tttatcgtca gctggcgcaa cccgaccaag 780 gcccagcgtg agtggggtct gtcgacttac atcgatgcgc tcaaagaagc cgtcgacgta 840 gtttccgcca tcaccggcag caaagacatc aacatgctcg gcgcctgctc cggtggcatt 900 acctgcaccg cgctgctggg tcactacgcc gctctcggcg agaagaaggt caatgccctg 960 acccttttgg tcagcgtgct cgacaccacc ctcgactccc aggttgcact gttcgtcgat 1020 gagaaaaccc tggaagctgc caagcgtcac tcgtatcagg ccggcgtgct ggaaggccgc 1080 gacatggcca aagtcttcgc ctggatgcgc cctaacgacc tgatctggaa ctactgggtc 1140 aacaactacc tgctgggtaa cgagccaccg gtcttcgaca ttcttttctg gaacaacgac 1200 accacccggt tgcctgctgc gttccacggc gatctgatcg aaatgttcaa aaataaccca 1260 ctggtgcgcg ccaatgcact cgaagtgagc ggcacgccga tcgacctcaa acaggtcact 1320 gccgacatct actccctggc cggcaccaac gatcacatca cgccctggaa gtcttgctac 1380 aagtcggcgc aactgttcgg tggcaaggtc gaattcgtgc tgtccagcag tgggcatatc 1440 cagagcattc tgaacccgcc gggcaatccg aaatcacgtt acatgaccag caccgacatg 1500 ccagccaccg ccaacgagtg gcaagaaaac tcaaccaagc acaccgactc ctggtggctg 1560 cactggcagg cctggcaggc cgagcgctcg ggcaaactga aaaagtcccc gaccagcctg 1620 ggcaacaagg cctatccgtc aggagaagcc gcgccgggca cgtatgtgca tgaacgttaa 1680 3 1826 DNA Pseudomonas 3 ctgcagtgct ctctgaacta gaaagcaacg ttgtgcaatt aacggtcacc cgagcagtag 60 tacctggcgg ttgctgtgtg actacacagc tggtcccggt actcgtctca ggacaatgga 120 gcgtcgtaga tgagtaacaa gaatagcgat gacttgaatc gtcaagcctc ggaaaacacc 180 ttggggctta accctgtcat cggcctgcgt ggaaaagatc tgctgacttc tgcccgaatg 240 gttttaaccc aagccatcaa acaacccatt cacagcgtca agcacgtcgc gcattttggc 300 atcgagctga agaacgtgat gtttggcaaa tcgaagctgc aaccggaaag cgatgaccgt 360 cgtttcaacg accccgcctg gagtcagaac ccactctaca aacgttatct acaaacctac 420 ctggcgtggc gcaaggaact ccacgactgg atcggcaaca gcaaactgtc cgaacaggac 480 atcaatcgcg ctcacttcgt gatcaccctg atgaccgaag ccatggcccc gaccaacagt 540 gcggccaatc cggcggcggt caaacgcttc ttcgaaaccg gcggtaaaag cctgctcgac 600 ggcctcacac atctggccaa ggacctggta aacaacggcg gcatgccgag ccaggtggac 660 atgggcgctt tcgaagtcgg caagagtctg gggacgactg aaggtgcagt ggttttccgc 720 aacgacgtcc tcgaattgat ccagtaccgg ccgaccaccg aacaggtgca tgagcgaccg 780 ctgctggtgg tcccaccgca gatcaacaag ttttatgtgt ttgacctgag cccggataaa 840 agcctggcgc gcttctgcct gagcaacaac cagcaaacct ttatcgtcag ctggcgcaac 900 ccgaccaagg cccagcgtga gtggggtctg tcgacttaca tcgatgcgct caaagaagcc 960 gtcgacgtag tttccgccat caccggcagc aaagacatca acatgctcgg cgcctgctcc 1020 ggtggcatta cctgcaccgc gctgctgggt cactacgccg ctctcggcga gaagaaggtc 1080 aatgccctga cccttttggt cagcgtgctc gacaccaccc tcgactccca ggttgcactg 1140 ttcgtcgatg agaaaaccct ggaagctgcc aagcgtcact cgtatcaggc cggcgtgctg 1200 gaaggccgcg acatggccaa agtcttcgcc tggatgcgcc ctaacgacct gatctggaac 1260 tactgggtca acaactacct gctgggtaac gagccaccgg tcttcgacat tcttttctgg 1320 aacaacgaca ccacccggtt gcctgctgcg ttccacggcg atctgatcga aatgttcaaa 1380 aataacccac tggtgcgcgc caatgcactc gaagtgagcg gcacgccgat cgacctcaaa 1440 caggtcactg ccgacatcta ctccctggcc ggcaccaacg atcacatcac gccctggaag 1500 tcttgctaca agtcggcgca actgttcggt ggcaaggtcg aattcgtgct gtccagcagt 1560 gggcatatcc agagcattct gaacccgccg ggcaatccga aatcacgtta catgaccagc 1620 accgacatgc cagccaccgc caacgagtgg caagaaaact caaccaagca caccgactcc 1680 tggtggctgc actggcaggc ctggcaggcc gagcgctcgg gcaaactgaa aaagtccccg 1740 accagcctgg gcaacaaggc ctatccgtca ggagaagccg cgccgggcac gtatgtgcat 1800 gaacgttaag ttgtaggcag tctaga 1826 4 24 DNA Artifical Sequence Synthetic DNA 4 ccscagatca acaagttyta sgac 24 5 1683 DNA Pseudomonas CDS (1)...(1683) 5 atg aga gag aaa cca acg ccg ggc ttg ctg ccc aca ccc gcg acg ttc 48 Met Arg Glu Lys Pro Thr Pro Gly Leu Leu Pro Thr Pro Ala Thr Phe 1 5 10 15 atc aac gct cag agt gcg att acc ggt ctg cgc ggc cgg gat ctg ttc 96 Ile Asn Ala Gln Ser Ala Ile Thr Gly Leu Arg Gly Arg Asp Leu Phe 20 25 30 tcg acc ctg cgc agc gtg gcc gcc cac ggc ctg cgt cac ccg gtg cgc 144 Ser Thr Leu Arg Ser Val Ala Ala His Gly Leu Arg His Pro Val Arg 35 40 45 agc gcc cgt cat gtt ctg gca ctg ggc ggc cag ttg ggc cgc gtg ctg 192 Ser Ala Arg His Val Leu Ala Leu Gly Gly Gln Leu Gly Arg Val Leu 50 55 60 ctg ggc gaa acg ctg cac acg ccg aac ccg aaa gac aat cgc ttt gcg 240 Leu Gly Glu Thr Leu His Thr Pro Asn Pro Lys Asp Asn Arg Phe Ala 65 70 75 80 gac ccg acc tgg aga ctg aat ccg ttt tac cgg cgc agc ctg cag gcc 288 Asp Pro Thr Trp Arg Leu Asn Pro Phe Tyr Arg Arg Ser Leu Gln Ala 85 90 95 tat ctg agc tgg cag aaa cag gtc aaa agc tgg atc gat gaa agc ggc 336 Tyr Leu Ser Trp Gln Lys Gln Val Lys Ser Trp Ile Asp Glu Ser Gly 100 105 110 atg agt gac gat gac cgc gcc cgc gcg cat ttc gtc ttc gca ctg ctc 384 Met Ser Asp Asp Asp Arg Ala Arg Ala His Phe Val Phe Ala Leu Leu 115 120 125 aat gac gcc gtg tcc ccc tcc aat acc ctg ctc aac ccg cta gcg atc 432 Asn Asp Ala Val Ser Pro Ser Asn Thr Leu Leu Asn Pro Leu Ala Ile 130 135 140 aag gag ctg ttc aac tcc ggt ggc aac agc ctg gtc cgc ggt ctc agc 480 Lys Glu Leu Phe Asn Ser Gly Gly Asn Ser Leu Val Arg Gly Leu Ser 145 150 155 160 cat tta ttc gac gac ctg atg cac aac aac ggg ctg ccc agt cag gtc 528 His Leu Phe Asp Asp Leu Met His Asn Asn Gly Leu Pro Ser Gln Val 165 170 175 acc aaa cac gcc ttc gag att ggc aag acc gtg gca acc acc gcc ggg 576 Thr Lys His Ala Phe Glu Ile Gly Lys Thr Val Ala Thr Thr Ala Gly 180 185 190 tcc gtg gtg ttt cgc aac gag ctg ctc gag ctg atg cag tac aag ccg 624 Ser Val Val Phe Arg Asn Glu Leu Leu Glu Leu Met Gln Tyr Lys Pro 195 200 205 atg agc gaa aaa cag tac gcc aag ccg ttg ctg atc gtc ccg ccg cag 672 Met Ser Glu Lys Gln Tyr Ala Lys Pro Leu Leu Ile Val Pro Pro Gln 210 215 220 att aac aag tac tac att ttc gac ctc agc ccg ggt aac agc ttc gtc 720 Ile Asn Lys Tyr Tyr Ile Phe Asp Leu Ser Pro Gly Asn Ser Phe Val 225 230 235 240 cag tac gca ttg aag aat ggt ctg cag gtg ttc gtg gtc agc tgg cgt 768 Gln Tyr Ala Leu Lys Asn Gly Leu Gln Val Phe Val Val Ser Trp Arg 245 250 255 aac ccg gat gtt cgc cac cgc gaa tgg ggc ctg tcc agt tac gtt gag 816 Asn Pro Asp Val Arg His Arg Glu Trp Gly Leu Ser Ser Tyr Val Glu 260 265 270 gca ctg gaa gaa gca ctg aat gtt tgc cgc gct atc acc ggc gcg cgc 864 Ala Leu Glu Glu Ala Leu Asn Val Cys Arg Ala Ile Thr Gly Ala Arg 275 280 285 gac gtc aat ctg atg ggc gcc tgt gct ggc ggc ctg acc atc gcg gct 912 Asp Val Asn Leu Met Gly Ala Cys Ala Gly Gly Leu Thr Ile Ala Ala 290 295 300 ctg caa ggt cat ctg caa gcc aag cgg caa ctg cgg cgg gtc tcc agc 960 Leu Gln Gly His Leu Gln Ala Lys Arg Gln Leu Arg Arg Val Ser Ser 305 310 315 320 gcc agc tac ctg gtc agc ctg ctg gat agc cag ata gac agc ccg gcg 1008 Ala Ser Tyr Leu Val Ser Leu Leu Asp Ser Gln Ile Asp Ser Pro Ala 325 330 335 acg ttg ttc gcc gat gag cag acg ctg gaa gcc gcc aag cgc cat tcc 1056 Thr Leu Phe Ala Asp Glu Gln Thr Leu Glu Ala Ala Lys Arg His Ser 340 345 350 tat caa cga ggt gtg ctc gag ggg cgc gac atg gcg aaa atc ttc gcc 1104 Tyr Gln Arg Gly Val Leu Glu Gly Arg Asp Met Ala Lys Ile Phe Ala 355 360 365 tgg atg cgc ccc aat gac ctg atc tgg aac tac tgg gtc aac aac tac 1152 Trp Met Arg Pro Asn Asp Leu Ile Trp Asn Tyr Trp Val Asn Asn Tyr 370 375 380 ctg ctg ggc aaa gaa ccg ccg gcc ttc gac att ctg tat tgg aac agt 1200 Leu Leu Gly Lys Glu Pro Pro Ala Phe Asp Ile Leu Tyr Trp Asn Ser 385 390 395 400 gac aac acg cgc ctg cca gcg gca ttc cat ggc gac ctg ctg gac ttc 1248 Asp Asn Thr Arg Leu Pro Ala Ala Phe His Gly Asp Leu Leu Asp Phe 405 410 415 ttc aag cac aat ccg ctg act cac ccc ggc ggg ctg gag gtc tgt ggc 1296 Phe Lys His Asn Pro Leu Thr His Pro Gly Gly Leu Glu Val Cys Gly 420 425 430 acg cct atc gat ttg cag aag gtc aac gta gac agc ttc agc gtg gcc 1344 Thr Pro Ile Asp Leu Gln Lys Val Asn Val Asp Ser Phe Ser Val Ala 435 440 445 ggc atc aac gac cac atc act ccg tgg gac gcg gtg tac cgc tcg acc 1392 Gly Ile Asn Asp His Ile Thr Pro Trp Asp Ala Val Tyr Arg Ser Thr 450 455 460 ctg ctg ctg ggt ggc gac cgg cgc ttc gta ctg tcc aac agc ggg cat 1440 Leu Leu Leu Gly Gly Asp Arg Arg Phe Val Leu Ser Asn Ser Gly His 465 470 475 480 atc cag agc atc ctc aac ccg ccg agc aac ccc aag tcc aac tac atc 1488 Ile Gln Ser Ile Leu Asn Pro Pro Ser Asn Pro Lys Ser Asn Tyr Ile 485 490 495 gag aac ccc aag ctc agt ggc gat cca cgc gcc tgg tat tac gac ggc 1536 Glu Asn Pro Lys Leu Ser Gly Asp Pro Arg Ala Trp Tyr Tyr Asp Gly 500 505 510 acc cat gtc gaa ggt agc tgg tgg cca cgt tgg ctg agc tgg att cag 1584 Thr His Val Glu Gly Ser Trp Trp Pro Arg Trp Leu Ser Trp Ile Gln 515 520 525 gag cgc tcc ggt acc caa cgc gaa acc ctg atg gcc ctt ggt aac cag 1632 Glu Arg Ser Gly Thr Gln Arg Glu Thr Leu Met Ala Leu Gly Asn Gln 530 535 540 aac tat cca ccg atg gag gcg gcg cca ggt acc tac gtg cgc gtg cgc 1680 Asn Tyr Pro Pro Met Glu Ala Ala Pro Gly Thr Tyr Val Arg Val Arg 545 550 555 560 tga 1683 * 6 560 PRT Pseudomonas 6 Met Arg Glu Lys Pro Thr Pro Gly Leu Leu Pro Thr Pro Ala Thr Phe 1 5 10 15 Ile Asn Ala Gln Ser Ala Ile Thr Gly Leu Arg Gly Arg Asp Leu Phe 20 25 30 Ser Thr Leu Arg Ser Val Ala Ala His Gly Leu Arg His Pro Val Arg 35 40 45 Ser Ala Arg His Val Leu Ala Leu Gly Gly Gln Leu Gly Arg Val Leu 50 55 60 Leu Gly Glu Thr Leu His Thr Pro Asn Pro Lys Asp Asn Arg Phe Ala 65 70 75 80 Asp Pro Thr Trp Arg Leu Asn Pro Phe Tyr Arg Arg Ser Leu Gln Ala 85 90 95 Tyr Leu Ser Trp Gln Lys Gln Val Lys Ser Trp Ile Asp Glu Ser Gly 100 105 110 Met Ser Asp Asp Asp Arg Ala Arg Ala His Phe Val Phe Ala Leu Leu 115 120 125 Asn Asp Ala Val Ser Pro Ser Asn Thr Leu Leu Asn Pro Leu Ala Ile 130 135 140 Lys Glu Leu Phe Asn Ser Gly Gly Asn Ser Leu Val Arg Gly Leu Ser 145 150 155 160 His Leu Phe Asp Asp Leu Met His Asn Asn Gly Leu Pro Ser Gln Val 165 170 175 Thr Lys His Ala Phe Glu Ile Gly Lys Thr Val Ala Thr Thr Ala Gly 180 185 190 Ser Val Val Phe Arg Asn Glu Leu Leu Glu Leu Met Gln Tyr Lys Pro 195 200 205 Met Ser Glu Lys Gln Tyr Ala Lys Pro Leu Leu Ile Val Pro Pro Gln 210 215 220 Ile Asn Lys Tyr Tyr Ile Phe Asp Leu Ser Pro Gly Asn Ser Phe Val 225 230 235 240 Gln Tyr Ala Leu Lys Asn Gly Leu Gln Val Phe Val Val Ser Trp Arg 245 250 255 Asn Pro Asp Val Arg His Arg Glu Trp Gly Leu Ser Ser Tyr Val Glu 260 265 270 Ala Leu Glu Glu Ala Leu Asn Val Cys Arg Ala Ile Thr Gly Ala Arg 275 280 285 Asp Val Asn Leu Met Gly Ala Cys Ala Gly Gly Leu Thr Ile Ala Ala 290 295 300 Leu Gln Gly His Leu Gln Ala Lys Arg Gln Leu Arg Arg Val Ser Ser 305 310 315 320 Ala Ser Tyr Leu Val Ser Leu Leu Asp Ser Gln Ile Asp Ser Pro Ala 325 330 335 Thr Leu Phe Ala Asp Glu Gln Thr Leu Glu Ala Ala Lys Arg His Ser 340 345 350 Tyr Gln Arg Gly Val Leu Glu Gly Arg Asp Met Ala Lys Ile Phe Ala 355 360 365 Trp Met Arg Pro Asn Asp Leu Ile Trp Asn Tyr Trp Val Asn Asn Tyr 370 375 380 Leu Leu Gly Lys Glu Pro Pro Ala Phe Asp Ile Leu Tyr Trp Asn Ser 385 390 395 400 Asp Asn Thr Arg Leu Pro Ala Ala Phe His Gly Asp Leu Leu Asp Phe 405 410 415 Phe Lys His Asn Pro Leu Thr His Pro Gly Gly Leu Glu Val Cys Gly 420 425 430 Thr Pro Ile Asp Leu Gln Lys Val Asn Val Asp Ser Phe Ser Val Ala 435 440 445 Gly Ile Asn Asp His Ile Thr Pro Trp Asp Ala Val Tyr Arg Ser Thr 450 455 460 Leu Leu Leu Gly Gly Asp Arg Arg Phe Val Leu Ser Asn Ser Gly His 465 470 475 480 Ile Gln Ser Ile Leu Asn Pro Pro Ser Asn Pro Lys Ser Asn Tyr Ile 485 490 495 Glu Asn Pro Lys Leu Ser Gly Asp Pro Arg Ala Trp Tyr Tyr Asp Gly 500 505 510 Thr His Val Glu Gly Ser Trp Trp Pro Arg Trp Leu Ser Trp Ile Gln 515 520 525 Glu Arg Ser Gly Thr Gln Arg Glu Thr Leu Met Ala Leu Gly Asn Gln 530 535 540 Asn Tyr Pro Pro Met Glu Ala Ala Pro Gly Thr Tyr Val Arg Val Arg 545 550 555 560 7 24 DNA Artifical Sequence Synthetic DNA 7 ccscagatca acaagttyta sgac 24 8 6029 DNA Pseudomonas 8 gaattcttgc gcgtgcactc tccttccgcc gaagtccagg gccacggcaa acctatcctg 60 caatttggca agatcggcgt aggcctgaac aaggtagaac cggccggtca gtacgcactg 120 aaattgacct tcgacgacgg ccatgacagc ggcctgttca cctgggatta tctgtaccaa 180 ctggcacaac gtcaggaagc actttgggca gattatcttg cagaactcaa agcggctgga 240 aagtcccgcg acccaagcga atccatcgtc aagctgatgc tctaattcag gcctcttgct 300 ctttagaggg cattttctaa tttcatctgt ttgaatgctc cgctgtgcgg caagcgattg 360 gcctgcttgc gaaaaaaatt aaactcgggt aaccaatgga gctggcaagt tccctgcagt 420 gctctctgaa ctagaaagca acgttgtgca attaacggtc acccgagcag tagtacctgg 480 cggttgctgt gtgactacac agctggtccc ggtactcgtc tcaggacaat ggagcgtcgt 540 agatgagtaa caagaatagc gatgacttga atcgtcaagc ctcggaaaac accttggggc 600 ttaaccctgt catcggcctg cgtggaaaag atctgctgac ttctgcccga atggttttaa 660 cccaagccat caaacaaccc attcacagcg tcaagcacgt cgcgcatttt ggcatcgagc 720 tgaagaacgt gatgtttggc aaatcgaagc tgcaaccgga aagcgatgac cgtcgtttca 780 acgaccccgc ctggagtcag aacccactct acaaacgtta tctacaaacc tacctggcgt 840 ggcgcaagga actccacgac tggatcggca acagcaaact gtccgaacag gacatcaatc 900 gcgctcactt cgtgatcacc ctgatgaccg aagccatggc cccgaccaac agtgcggcca 960 atccggcggc ggtcaaacgc ttcttcgaaa ccggcggtaa aagcctgctc gacggcctca 1020 cacatctggc caaggacctg gtaaacaacg gcggcatgcc gagccaggtg gacatgggcg 1080 ctttcgaagt cggcaagagt ctggggacga ctgaaggtgc agtggttttc cgcaacgacg 1140 tcctcgaatt gatccagtac cggccgacca ccgaacaggt gcatgagcga ccgctgctgg 1200 tggtcccacc gcagatcaac aagttttatg tgtttgacct gagcccggat aaaagcctgg 1260 cgcgcttctg cctgagcaac aaccagcaaa cctttatcgt cagctggcgc aacccgacca 1320 aggcccagcg tgagtggggt ctgtcgactt acatcgatgc gctcaaagaa gccgtcgacg 1380 tagtttccgc catcaccggc agcaaagaca tcaacatgct cggcgcctgc tccggtggca 1440 ttacctgcac cgcgctgctg ggtcactacg ccgctctcgg cgagaagaag gtcaatgccc 1500 tgaccctttt ggtcagcgtg ctcgacacca ccctcgactc ccaggttgca ctgttcgtcg 1560 atgagaaaac cctggaagct gccaagcgtc actcgtatca ggccggcgtg ctggaaggcc 1620 gcgacatggc caaagtcttc gcctggatgc gccctaacga cctgatctgg aactactggg 1680 tcaacaacta cctgctgggt aacgagccac cggtcttcga cattcttttc tggaacaacg 1740 acaccacccg gttgcctgct gcgttccacg gcgatctgat cgaaatgttc aaaaataacc 1800 cactggtgcg cgccaatgca ctcgaagtga gcggcacgcc gatcgacctc aaacaggtca 1860 ctgccgacat ctactccctg gccggcacca acgatcacat cacgccctgg aagtcttgct 1920 acaagtcggc gcaactgttc ggtggcaagg tcgaattcgt gctgtccagc agtgggcata 1980 tccagagcat tctgaacccg ccgggcaatc cgaaatcacg ttacatgacc agcaccgaca 2040 tgccagccac cgccaacgag tggcaagaaa actcaaccaa gcacaccgac tcctggtggc 2100 tgcactggca ggcctggcag gccgagcgct cgggcaaact gaaaaagtcc ccgaccagcc 2160 tgggcaacaa ggcctatccg tcaggagaag ccgcgccggg cacgtatgtg catgaacgtt 2220 aagttgtagg cagtctagaa gtccgcggca ctcggaggtg ccgcgagccc taccccatac 2280 agccgaggcc aggcctcgag taatctggag cacgctcagg acggcgtgtc cggcggttta 2340 acccacaggg cttctgagat gccgcaaccg ttcatattcc gtactgtcga cctggatggc 2400 caaaccatcc gcaccgcagt acgccccggc aagtctcata tgacgccctt gcttattttc 2460 aatggcatcg gcgccaacct ggagctggcg ttcccgttcg tccaggcgct tgacccggac 2520 ctggaggtga ttgccttcga cgttcccggt gttggcggct catcgacgcc cagcatgcct 2580 taccgctttc ccagtctggc caagctgacc gcgcgcatgc tcgactacct ggactacggg 2640 caagtcaacg tcgtgggcgt ttcctggggt ggagcactgg cccagcagtt tgcttacgac 2700 tatccagagc gctgcaaaaa actggtgctt gcggcaaccg cggcaggctc ctttatggtg 2760 ccgggcaagc cgaaagtgct gtggatgatg gcaagcccca ggcgctatat ccagccctcc 2820 catgtgattc gcattgctcc gctgatctat ggcggatcct tccgtcgcga ccccaatctg 2880 gccgcagaac acgccagcaa agtacgttcg gccggcaagc tgggttacta ctggcagctg 2940 ttcgcgggtc tgggctggac cagcattcat tggctgcaca aaattcatca gcccaccctg 3000 gtgctggccg gtgacgacga cccgctgatc ccgctgatca acatgcgcat gctggcctgg 3060 cgaattccca acgcccagct acacataatc gacgatggtc atttgttcct gattacccgc 3120 gccgaagccg ttgcgccgat catcatgaag tttcttcagg aggagcgtca gcgggcagtg 3180 atgcatccgc acccgacgcc gctcggcaga acttagagtc tcgcggatgt tgaaaggacc 3240 ttcgcctgcg caagaacggg ctggaccgac tatggtgtct gtcttgaatt gatgtgcttg 3300 ttgatggctt gacgaaggag tgttgactca tgagagagaa accaacgccg ggcttgctgc 3360 ccacacccgc gacgttcatc aacgctcaga gtgcgattac cggtctgcgc ggccgggatc 3420 tgttctcgac cctgcgcagc gtggccgccc acggcctgcg tcacccggtg cgcagcgccc 3480 gtcatgttct ggcactgggc ggccagttgg gccgcgtgct gctgggcgaa acgctgcaca 3540 cgccgaaccc gaaagacaat cgctttgcgg acccgacctg gagactgaat ccgttttacc 3600 ggcgcagcct gcaggcctat ctgagctggc agaaacaggt caaaagctgg atcgatgaaa 3660 gcggcatgag tgacgatgac cgcgcccgcg cgcatttcgt cttcgcactg ctcaatgacg 3720 ccgtgtcccc ctccaatacc ctgctcaacc cgctagcgat caaggagctg ttcaactccg 3780 gtggcaacag cctggtccgc ggtctcagcc atttattcga cgacctgatg cacaacaacg 3840 ggctgcccag tcaggtcacc aaacacgcct tcgagattgg caagaccgtg gcaaccaccg 3900 ccgggtccgt ggtgtttcgc aacgagctgc tcgagctgat gcagtacaag ccgatgagcg 3960 aaaaacagta cgccaagccg ttgctgatcg tcccgccgca gattaacaag tactacattt 4020 tcgacctcag cccgggtaac agcttcgtcc agtacgcatt gaagaatggt ctgcaggtgt 4080 tcgtggtcag ctggcgtaac ccggatgttc gccaccgcga atggggcctg tccagttacg 4140 ttgaggcact ggaagaagca ctgaatgttt gccgcgctat caccggcgcg cgcgacgtca 4200 atctgatggg cgcctgtgct ggcggcctga ccatcgcggc tctgcaaggt catctgcaag 4260 ccaagcggca actgcggcgg gtctccagcg ccagctacct ggtcagcctg ctggatagcc 4320 agatagacag cccggcgacg ttgttcgccg atgagcagac gctggaagcc gccaagcgcc 4380 attcctatca acgaggtgtg ctcgaggggc gcgacatggc gaaaatcttc gcctggatgc 4440 gccccaatga cctgatctgg aactactggg tcaacaacta cctgctgggc aaagaaccgc 4500 cggccttcga cattctgtat tggaacagtg acaacacgcg cctgccagcg gcattccatg 4560 gcgacctgct ggacttcttc aagcacaatc cgctgactca ccccggcggg ctggaggtct 4620 gtggcacgcc tatcgatttg cagaaggtca acgtagacag cttcagcgtg gccggcatca 4680 acgaccacat cactccgtgg gacgcggtgt accgctcgac cctgctgctg ggtggcgacc 4740 ggcgcttcgt actgtccaac agcgggcata tccagagcat cctcaacccg ccgagcaacc 4800 ccaagtccaa ctacatcgag aaccccaagc tcagtggcga tccacgcgcc tggtattacg 4860 acggcaccca tgtcgaaggt agctggtggc cacgttggct gagctggatt caggagcgct 4920 ccggtaccca acgcgaaacc ctgatggccc ttggtaacca gaactatcca ccgatggagg 4980 cggcgccagg tacctacgtg cgcgtgcgct gaattctctc tgcaccacgg tcgggctatt 5040 ggccgtggca tgactcaata accaagaaga ctggatgaaa acccgcgacc ggatcctcga 5100 atgtgccctg caactgttca accaaaaggg cgaaccgaat gtctccacca tggaagttgc 5160 caatgagatg ggcatcagcc ctggcaacct ctattaccac tttcatggca aggaaccgct 5220 gatcctcggc ttgttcgagc gcttccaggc cgaactggtc ccgctgctcg acccgccggc 5280 ggacgtacaa ctggccgctg gagattattg gctgttcctg cacctgatcg tcgagcgcct 5340 ggcgcactac cgcttcctgt ttcaggacct gtccaacctg gccggacgct taccgaaact 5400 ggccaagggc attcgcaacc tgctcaatgc cttgaagcgt accctggcgt cgttgttggc 5460 gcggttgaaa gcgcaaggac agttggtcag cgacacacag gcgctggggc aactggtcga 5520 gcagatcacc atgacgctgc tgttttcact cgactatcaa aggattcttg atcgcgaggg 5580 agaagtgcgg gtggtggtgt accagatcat gatgctggta gcgccgcacc tgctgccacc 5640 ggtgaaattg gcgacggagc aaatggcgtt gcgatatctg gaggagcatg agtgagagag 5700 ctgagtagga caccagatcg tttcctcgct gatgatcgtt cccacgcgcc gcaaaggaat 5760 gcagcccgtg acgctccgcg tcacaaaagc ggacgcagag cgtccagtga ggcattccca 5820 cgcgggagcg tgggaacgat caattttccg tcagaaacaa aaatgcccga catttacagg 5880 ccgggcgttt ttgtgagccc cgaaaaatca ggactgattg gttggcgtcg gtgaagtcgg 5940 cgcaacagtc ggggtaaccg caggggtcgg tgcagcagcg gagttcgctg tgctgaccgg 6000 agctgcgggg ttggccgcag caactgcag 6029 

What is claimed is:
 1. An isolated polynucleotide encoding a polypeptide comprising the amino acid sequence shown in SEQ ID NO:
 6. 2. An isolated polynucleotide selected from the group consisting of: a) SEQ ID NO: 5; b) SEQ ID NO: 5, wherein T is U; and c) nucleic acid sequences comlementary to a) to b).
 3. An isolated polynucleotide selected from the group consisting of: a) SEQ ID NO: 8; b) SEQ ID NO: 8 wherein T is U; and c) nucleic acid sequences complementary to a) or b).
 4. A vector containing a polynucleotide of claims 1, 2 or
 3. 5. The vector of claim 4, wherein the vector is a viral vector.
 6. The vector of claim 4, wherein the vector is a plasmid.
 7. A host cell containing a vector of claim
 4. 8. The host cell of claim 7, cultured under conditions which allow expression of the polynucleotide.
 9. A method for producing polyester synthase comprising: (a) culturing the host cell of claim 7 under conditions suitable for expression of said polyester synthase; and (b) recovering the polyester synthase accumulated in the culture medium, a body of the host cell or both of them. 